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Review Paper Role of Biochemical factors and Mineral Supplementation in Livestock ration for Maintenance of their Fertility and Healthy Reproductive Status: A Review

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Review Paper

Role of Biochemical factors and Mineral Supplementation in Livestock

ration for Maintenance of their Fertility and Healthy Reproductive Status:

A Review

Ganguly Subha

AICRP on Post Harvest Technology (ICAR), Department of Fish Processing Technology, Faculty of Fishery Sciences, West Bengal University of Animal and Fishery Sciences, 5, Budherhat Road, P.O. Panchasayar, Chakgaria, Kolkata - 700 094, WB, INDIA

Available online at: www.isca.in

Received 27th May 2013, revised 12th June 2013, accepted 16th June 2013

Abstract

The biochemical components and factors like protein and enzyme components of follicular fluid like lipase, amylase and creatinine phosphokinase concentration show an increasing trend as the follicles mature, while some other components like Alpha-fetoprotein, Acid Phosphatase and Alkaline Phosphatase concentration decreases with increase in follicular size. Moreover, presence of amylase, lipase and CPK and their respective concentrations in the in the follicular fluid can also been detected. The micro-minerals play an important role in increasing pregnancy rates in apparently barren and reproductively abnormal mares. Provision of micro-mineral supplemented ration containing copper, zinc, iron and manganese during the vernal period of breeding cycle proves to be useful. The pregnancy rate increase significantly in micro-mineral supplemented livestock. Some mineral components of follicular fluid like Ca, P, Cu and Fe significantly increases as the follicles increase in size, while only Li, concentration significantly decreases with increase in follicular size. Therefore, it may enhance more success in reproduction, which may improve the certain macro- and micro-mineral level in follicular fluid of oocytes.

Keywords: Biochemical factors, fertility, livestock, reproduction.

Introduction

Follicular fluid where oocytes grow and mature is a mixture of serum exudates and locally produced metabolites of follicular cells1 and is found in an avascular compartment within the ovarian follicle. Incorporation of follicular fluid into culture medium showed encouraging results in in-vitro maturation and fertilization of oocytes2,3. Alpha-fetoprotein, amylase, lipase and creatinine kinase remains present in FF. The present article is constructed to highlight the importance of quantitative biochemical estimation of different proteins like total protein, albumin, globulin and Alpha-fetoprotein and enzymes like alkaline phosphatase, acid phosphatase, lipase, amylase, creatinine kinase concentrations of FF harvested from ovarian follicles.The accurate diagnosis of mineral deficiency is revealed by clinical and production response4. Old mares have lower pregnancy rates per cycle and increased pregnancy loss rates5. Deficiency of minerals causes various reproductive failures such as infertility, repeat breeding, embryonic loss, poor conception rate, anestrous condition etc6. The influence of micro-minerals on reproductive efficiency, ovulatory mechanism and maintenance of pregnancies and regulation of endocrine functions in the animals is important7.

Investigation reports and research findings

Proteins in the living cells are intimately associated with various phases of activity that constitute the life of the cells8. The

gradual decrease in the concentration of total protein, albumin and globulin in the different sized follicles is related with estrogen and water uptake in growing follicles and due to this water uptake there is dilution of follicular protein concentration. It was observed that total protein concentrations in small, medium, and large sized goat ovarian follicular fluid were 84.24%, 69.16%, and 71.02% of total protein of serum, respectively9,10. A number of proteins reside in follicular fluid and surrounding granulosa cells, therefore, a small change in hydration could produce large effects on protein concentrations as follicles were growing11.

Developing follicles need amino acids for their activity. Ovary is one of the most active tissue in catabolizing albumin12.There is active inward transport of albumin from blood into follicles which may be required for binding some chemicals as well as minerals inside the follicular fluid for various physiological functions including growth and maturation of follicles13.

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maturation and programmingof the positive feedback exerted by ovary-derived estrogen on brain LH and FSH levels.15 Physiological studies on AFP-estrogen interaction revealed rat Alpha-feto protein was able to inhibit the formation of water-soluble metabolites of E2 and E1, when microsomes from rat

liver were incubated in the presenceof NADPH, and to regulate the activity of 17β-hydroxy steroid dehydrogenase in vitro16. AFP has also beenassociated with the delay in the onset of puberty in postnatalrat pups17. The injection of AFP during the prepubertalperiod in rats has resulted in a decreased number of primordialand primary follicles in the ovary18.

The changes in enzymatic activity of ACP have an important role in ovulation, and it seems that there is relationship between its presence and oocyte fertilization by spermatozoon19. However, ACP may be important for steroidogenesis. Phosphatase enzymes were implicated in both growth and atresia of follicles. A progressive decrease in the ACP and ALP activity with follicular maturation was noted.

ALP and ACP are lysosomal enzymes which catalyze various reactions in the body and are involved in the active transport of protein and DNA turnover in nucleus.20 The higher alkaline phosphatase activity in the initial stages of follicular development might be due to a progesterone and androgen dominant environment that exits in the small follicle, in that a higher concentration of progesterone and androgen could be conducive to phosphatase activity21. The decreased follicular fluid alkaline phosphatase activity with the development of the follicle could be due to the shift in the follicular hormonal milieu from androgen to estrogen dominance, with the development of the follicle. Thus, the changes in the phosphatase activity could reflect changes in metabolic activity on tissue synthesis mechanisms induced by the different hormones.

The role of the endothelial-bound lipases in ovarian physiology is largely unknown. The ovary is metabolically very active organ that needs fatty acids as energy substrate for synthesis of lipid mediators and cholesterol for hormone synthesis. The rat ovary has been shown to be highly dependent on oxidation of

fatty acids for the generation of adenosine 5’-triphosphate for

energy metabolism, growth, and steroidogenesis22,23.The lipase

would facilitate the supply of fatty acids from lipoproteins to cells of several parts of the ovary, including the corpus luteum and the growing follicle with its enclosed oocyte and the avascular granulosa layer.

Lipases bound to the luminal side of the vascular endothelium

may thus be the first in line among several mechanisms

facilitating the uptake of fatty acids andcholesterol by ovarian

cells24.

Alpha- amylase activity in ovarian tissue was more during proestrus when follicular size was large and low in diestrus when follicular size was small, because follicular fluid is

partially derived from ovarian epithelium.25 Kasperczyk et al.25 also suggested that change of amylase concentration might be due to action of sex hormones on ovarian tissues.

According to Malnick et al.26, brain-type isozyme of creatinine kinase (CKBB) responds to estrogen in female reproductive tract. Chang et al.27 reported that estrogen concentration increased as follicular size increased in pig.

Higher serum copper level in normal mares than in apparently barren animals was observed by Joy and Nair28 and Prasad and Rao29. Prasad and Rao29 and Kalita et al.30found significantly low serum zinc level in repeat breeding animals. Increased serum iron level in apparently barren animals was reported by Eltohamy et al.31 and Singh and Pant32. The higher concentration of serum manganese level was observed by Eltohamy et al.31 and Prasad and Rao29 respectively.

Islam et al.7 carried out a study to determine the role of micro-minerals in increasing pregnancy rates in apparently barren and reproductively normal mares. For this study, normal healthy mares and apparently barren (infertile) mares were selected randomly and were subjected to micro-mineral supplemented ration containing copper, zinc, iron and manganese for 20 days during their vernal period of breeding cycle. After the investigation, it was found that the pregnancy rate in micro-mineral supplemented group was significantly higher (P<0.05) than in non-supplemented group. It was evident that pregnancy rate in supplemented group of apparently barren mares was 55.56%, while in non-supplemented group was 33.33%. The pregnancy rate in supplemented group of normal healthy mares was 60% while in non-supplemented group of normal mares was 50%.7

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The injected rat alpha-fetoprotein was localized to the zona pellucida of follicles undergoing atresia. Although, physiological role of AFP remains an enigma, its presence was found in FF and this study demonstrated that AFP was not only present in porcine FF but its concentration decreased significantly (p<0.01) with the development of follicles. However, the functions of AFP in FF remain to be investigated.

Lipase activity in this study found to be highest in large follicular fluid and lowest in small follicular fluid. Amylase activity in this study found to be highest in large follicular fluid and lowest in small follicular fluid. In the present study, CK concentration was found significantly higher in large follicles than in the medium follicles8.

Ca is one of the macro-minerals which play a major role in reproduction; its deficiency can affect fertility33. Marketa et al.34 have stated that free Ca ions seem to be involved in the regulation of oocyte growth and meiosis restoration at the beginning of oocyte maturation. Abd Ellah et al.35 analysed P concentration in buffalo follicular fluid, the findings of which was in support of the present study. The higher concentrations of Mg in the small follicles could help the mitosis of the follicular cells through the formation of thrombin, a potent mitogen. Magnesium could substitute for calcium in thrombin formation under low Ca:Mg ratio conditions, that exist in small follicles. As magnesium was antagonistic to calcium, the decreased magnesium with follicular development facilitated the calcium action in large follicles36. Magnesium acts as a cofactor in enzymatic reaction, and induces meiotic maturation of xenopus oocyte37.

Fe concentration in follicular fluid was significantly higher (p≤0.01) in large follicles than small and medium follicles. Increased Fe concentration in the developed follicles was due to the increased level of steroid hormones, which induce increased hemodynamic pulses and vascular shunt of the developing follicles38. Guraya et al.39 suggested that the variations in Fe content were in accordance with the hemodynamic changes observed in follicular wall during follicular development and maturation and these changes were regulated by intrafollicular factors. Bagger et al.40 in their study on mice found that Li enhanced the capability of mouse oocyte for continuation of meiosis by activation of cyclic AMP second massager path in the cumulus cells.

The concentration of all the macro- and micro-minerals in the porcine follicular fluid either increased or decreased with increase in follicular size, but only Ca, P, Cu and Fe concentrations significantly increased and only Li significantly decreased in follicular fluid. The change of concentration of Li in different sized follicular fluid might be related to folliculogenesis, and particularly maturation of follicles. Cumulus cells induce follicular cells to synthesize a meiosis inducing substance which stimulates the oocyte to resume meiosis41.

Conclusion

Mineral supplementation at appropriate concentrations can improve the pregnancy rates by reducing the incidences of repeat breeding in breeding livestock. So, optimum formulation of livestock ration mixed with adequate quantity of macro- and micro-minerals proves a stimulating factor in maintenance of pre- and post-pubertal stages in livestock. It also proves to be helpful in remediation of cases of silent heat, infertility, sterility and other reproductive disorders.

References

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11. Rupley J.A., Gratton E. and Carei G., Water and Globular Proteins, Trends Biochem. Science, 8, 18 (1983)

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17. Greenstein B.D., Effects of rat alpha-fetoprotein administration on estradiol free fraction, the onset of puberty, and neural and uterine nuclear estrogen receptors, Endocrinology, 130, 3184–90 (1992)

18. Stora C., Aussel C., Lafaurie M., Castelli D. and Seralini G.E., Role of AFP in ovarian regulation. In: Mizejewski G.J. and Jacobson H.I., Eds. Biological Activities of Alpha-fetoprotein, Boca Raton, CRC Press, 1, 112–20 (1987)

19. Gonzalez D.M., Garcia L.A., Nava Y., Lara E., Rosendo B.J. and Gomez A.E., Changes in follicular acid phosphatase levels in relation to oocyte maturity in humans, Ginecol. Obstet. Mex., 57, 37-40 (1989)

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26. Malnick S.D.H., Shaer A., Soreq H. Kaye A.M. and Litwack G., Estrogen-induced creatine kinase in the reproductive system of the immature female rat, Endocrinology, 113(5), 1907-09 (1983)

27. Chang S.C.S., Jones J.D., Ellefson R.D. and Ryan R.J., The porcine ovarian follicle: I. selected chemical analysis of follicular fluid at different developmental stages, Biological Reproduction, 15, 321-28 (1976)

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29. Prasad K.S.N. and Rao S.V.N., Blood mineral profile of anestrous and repeat breeders crossbred cows-a field study, Indian J. Anim. Nutr., 14 (2), 135-37 (1997)

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maturation of xenopus oocyte, Cell Differentiation, 19, 253-61 (1986)

38. Sangha G.K., Sharma R.K. and Guraya S.S., Distribution of trace elements in blood and ovary during estrous cycle and pregnancy in house rat, Indian Journal of Animal Science, 63(2), 142-45 (1993)

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References

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